Copper foil with carrier, coreless support with wiring layer, and method for producing printed circuit board

ABSTRACT

There is provided a copper foil provided with a carrier exhibiting a high peeling resistance against the developer in the photoresist developing process and achieving high stability of mechanical peel strength of the carrier. The copper foil provided with a carrier comprises a carrier; an interlayer disposed on the carrier, the interlayer having a first surface adjacent to the carrier and containing 1.0 atom % or more of at least one metal selected from the group consisting of Ti, Cr, Mo, Mn, W and Ni and a second surface remote from the carrier and containing 30 atom % or more of Cu; a release layer disposed on the interlayer; and an extremely-thin copper layer disposed on the release layer.

CROSS-REFERENCE TO RELATED APPLICATIONS

The present application is a Continuation of U.S. application Ser. No. 16/397,449, filed Apr. 29, 2019, which is a Continuation of U.S. application Ser. No. 16/080,442, filed Aug. 28, 2018, now issued as U.S. Pat. No. 10,356,915, which is a National stage of International Patent Application No. PCT/JP2017/006423, filed Feb. 21, 2017, which claims priority to International Patent Application No. PCT/JP2016/076047, filed Sep. 5, 2016 and Japanese Application No. 2016-037308, filed Feb. 29, 2016. The disclosure of each of these applications is incorporated by reference herein in its entirety.

TECHNICAL FIELD

The present invention relates to a copper foil provided with a carrier and a method for manufacturing a coreless support provided with a wiring layer and a printed wiring board.

BACKGROUND ART

In recent years, multilayer printed wiring boards have gradually prevailed to meet a decrease in size of and an increase in packaging density on the printed wiring board. Such multilayer printed wiring boards have been used for reductions in weight and size of many portable electronic devices. Requirements for the multilayer printed wiring boards include a further reduction in thickness of the insulating interlayer and a further reduction in weight of the wiring board itself.

To meet such requirements, a method for manufacturing a multilayer printed wiring board by a coreless build-up process has been employed. The coreless build-up process alternately builds up insulating layers and wiring layers without a so-called core substrate into a multilayer. In the coreless build-up process, it has been proposed to use a copper foil provided with a carrier to facilitate separation between the support and the multilayer printed wiring board. For example, Patent Document 1 (JP2005-101137A) discloses a method for manufacturing a package substrate for mounting semiconductor devices, comprising bonding an insulating resin layer to the carrier surface of a copper foil provided with a carrier to form a support and then forming a first wiring conductor adjacent to the extremely-thin copper layer of the copper foil provided with a carrier by a process, for example, photoresist processing, pattern electrolytic copper plating, or resist removal, followed by forming a build-up wiring layer, releasing the supporting substrate provided with a carrier, and removing the extremely-thin copper layer.

Meanwhile, a copper foil provided with a carrier having an extremely-thin copper layer having a thickness of 1 μm or less has been desired to miniaturize the embedded circuit as shown in Patent Document 1. Accordingly, it has been proposed to form an extremely-thin copper layer by vapor deposition to achieve a reduction in thickness of the extremely-thin copper layer. For example, Patent Document 2 (JP4726855B2) discloses a copper foil with a carrier sheet interposed by a bonding interface layer. The bonding interface layer consists of two sublayers, i.e., a metal sublayer (adjacent to the carrier sheet) and a carbon sublayer (adjacent to the extremely-thin copper layer) and the copper foil layer was prepared by forming a first copper layer having a thickness of 10 nm to 300 nm on the bonding interface layer by physical vapor deposition and further forming a second copper layer by electrolysis. This document also discloses that the metal sublayer of the bonding interface layer may be composed of any one of tantalum, niobium, zirconium, nickel, chromium, titanium, iron, silicon, molybdenum, vanadium, and tungsten.

Patent Document 3 (JP4072431) discloses a copper foil provided with a carrier having a surface provided with, in sequence, a chromium release layer, an antidiffusion layer readily absorbable light having wavelengths oscillated by CO₂ gas laser, and an electrolytic copper plating layer, wherein the antidiffusion layer is a single-metal layer composed of an element selected from the group consisting of nickel, cobalt, iron, molybdenum, tungsten, aluminum, and phosphorus, or an alloy layer composed of two or more elements selected from the group consisting of nickel, cobalt, iron, chromium, molybdenum, tungsten, copper, aluminum and phosphorus or a metal oxide layer of one or more elements.

CITATION LIST Patent Documents

Patent Document 1: JP2005-101137A

Patent Document 2: JP4726855B2

Patent Document 3: JP4072431B2

Patent Document 4: JP2015-35551

SUMMARY OF INVENTION

Meanwhile, the use of a coreless build-up method is also examined in Fan-Out Wafer Level Packaging (FO-WLP) and Fan-Out Panel Level Packaging (FO-PLP), which are packaging technologies for printed wiring boards. A Redistribution Layer-First (RDL-First) method is one of the packaging technologies (see, for example, Patent Document 4 (JP2015-35551A) that involves forming a wiring layer and a build-up wiring layer, as required, on the surface of a coreless support, releasing the support as required, and then mounting the chip. This method enables image inspection of the wiring layer on the surface of the coreless support and each build-up wiring layer stacked thereafter before chip mounting, so that the chip may be mounted only on non-defective portion of each wiring layer. As a result, the RDL-First method, which does not cause wasteful use of the chip, is economically advantageous compared to the Chip-First method, which sequentially stacks the wiring layer on the surface of the chip. Image inspection immediately after the wiring layer is formed on the surface of the coreless support involves processes such as photoresist processing, electroplating, and photoresist peeling on the surface of the coreless support, flash etching of the extremely-thin copper layer existing between the wirings as necessary, followed by mounting of electronic elements such as chips as necessary, resulting in build-up layer. Mount of an electronic element such as a chip, however, involves heating, so that coreless support likely to warp. To prevent this problem, materials such as glass, ceramics, and low thermal expansion resins which have a low thermal expansion coefficient (CTE) are considered to be used as carriers. Unfortunately, carriers composed of such a low thermal expansion material are likely to peel off readily. This problem is especially noticeable in the case of a carbon release layer. Although a possible countermeasure is to provide a layer for improving adhesion between the release layer and the carrier, it causes the peel strength of the carrier to be unstable, precluding stable removal of the carrier at the time of separation of the coreless support. Thus, stable mechanical peel strength of the carrier cannot be achieved. In other words, the mechanical peel strength of the carrier is unstable. Meanwhile, another requirement on the copper foil provided with a carrier is to exhibit peeling resistance in a photoresist developing step (for example, a step using an aqueous sodium carbonate developer) for forming a wiring layer on the surface of the coreless support.

The inventors have found that an interlayer composed of a specific metal, which is interposed between the carrier and the release layer of the copper foil provided with a carrier, can provide a copper foil provided with a carrier exhibiting a high peeling resistance against the developer in the photoresist developing process and achieving high stability of mechanical peel strength of the carrier.

Accordingly, an object of the present invention is to provide a copper foil provided with a carrier exhibiting a high peeling resistance against the developer in the photoresist developing process and achieving high stability of mechanical peel strength of the carrier.

According to an aspect of the present invention, there is provided a copper foil provided with a carrier, comprising:

-   -   a carrier;     -   an interlayer disposed on the carrier, the interlayer having a         first surface adjacent to the carrier and containing 1.0 atom %         or more at least one metal selected from the group consisting of         Ti, Cr, Mo, Mn, W and Ni and a second surface remote from the         carrier and containing 30 atom % or more of Cu;     -   a release layer disposed on the interlayer; and     -   an extremely-thin copper layer disposed on the release layer.

According to another aspect of the present invention, there is provided a method for manufacturing a coreless support provided with a wiring layer, comprising the steps of:

-   -   providing the copper foil provided with a carrier according to         the above aspect as a support;     -   forming a photoresist layer with a predetermined pattern on the         surface of the extremely-thin copper layer;     -   forming an electrolytic copper plating layer on the exposed         surface of the extremely-thin copper layer;     -   peeling off the photoresist layer; and     -   removing an unnecessary portion of the extremely-thin copper         layer by copper flash etching to prepare a coreless support         provided with a wiring layer.

According to another aspect of the present invention, there is provided a method for manufacturing a printed wiring board, comprising the steps of:

-   -   manufacturing a coreless support provided with a wiring layer by         the method according to the above aspect,     -   forming a build-up layer on a surface having the wiring layer of         the coreless support provided with a wiring layer to prepare a         laminate with a build-up layer;     -   separating the laminate with a build-up layer at the release         layer to prepare a multilayer wiring board including the         build-up layer; and     -   processing the multilayer wiring board to prepare a printed         wiring board.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 is a schematic cross-sectional diagram illustrating an embodiment of a copper foil provided with a carrier of the present invention.

FIG. 2 is a schematic cross-sectional diagram illustrating another embodiment of a copper foil provided with a carrier of the present invention.

FIG. 3 is a process flow chart for explaining initial steps (steps (a) to (c)) of a method for manufacturing a coreless support provided with a wiring layer or a printed wiring board of the present invention.

FIG. 4 is a process flow chart for explaining middle steps (steps (d) to (f)) following FIG. 3 of a method for manufacturing a coreless support provided with a wiring layer or a printed wiring board of the present invention.

FIG. 5 is a process flow chart for explaining final steps (steps (g) to (i)) following FIG. 4 of a method for manufacturing a printed wiring board of the present invention.

DESCRIPTION OF EMBODIMENT

Copper Foil Provided with a Carrier

The copper foil provided with a carrier of the present invention is schematically illustrated in FIG. 1. As shown in FIG. 1, the copper foil 10 provided with a carrier of the present invention includes a carrier 12, an interlayer 14, a release layer 16, and an extremely-thin copper layer 18 in this order. The interlayer 14 is disposed on the carrier 12 and has a first surface adjacent to the carrier 12 and a second surface remote from the carrier 12. The first surface contains 1.0 atom % or more of at least one metal selected from the group consisting of Ti, Cr, Mo, Mn, W and Ni and the second surface contains 30 atom % or more of Cu. The release layer 16 is disposed on the interlayer 14. The extremely-thin copper layer 18, which is made of copper, is disposed on the release layer 16. The copper foil 10 provided with a carrier of the present invention may further include an optional antireflective layer 17 between the release layer 16 and the extremely-thin copper layer 18. These layers may be laminated on the upper and lower surfaces of the carrier 12 to be symmetric about the carrier 12. The copper foil 10 provided with a carrier may have any known layer configuration with proviso that the copper foil 10 provided with carrier is provided with the interlayer 14 and the optional antireflective layer 17.

Thus, a copper foil 10 provided with a carrier, including an interlayer 14 composed of a predetermined metal interposed between the carrier 12 and the release layer 16, can provide high peeling resistance against the developer in photoresist developing process, high stability of mechanical peel strength of the carrier, and excellent wiring pattern forming ability due to no detachment of the interlayer when the coreless support or the carrier is peeled off. Although the mechanism on such effect of the interlayer 14 is not clear, the inventors can propose the following reason. Copper constituting the surface remote from the carrier 12 (i.e., adjacent to the release layer 16) of the interlayer 14 can provide a stable releasability due to its lower adhesion to the material (for example, carbon) constituting the release layer 16, but can provide an unstable adhesion and releasability between the surface and the carrier (for example, glass or ceramics). In this respect, it is believed that 1.0 atom % or more of at least one metal selected from the group consisting of Ti, Cr, Mo, Mn, W and Ni contained on the surface (adjacent to the carrier 12) of the interlayer 14 can provide advantageously excellent release stability and peeling resistance against the developer between the interlayer 14 and the carrier 12.

The material of the carrier 12 may be any one of glass, ceramic, resin, and metal. Furthermore, the form of the carrier 12 may be any one of sheet, film, plate, and foil. Furthermore, the carrier 12 may be a laminate of materials such as sheets, films, plates, and foils. For example, the carrier 12 may function as a rigid support such as a glass plate, a ceramic plate, and a metal plate, or may be in a nonrigid support such as a metal foil or a resin film. Examples of the preferred metal of the carrier 12 include copper, titanium, nickel, stainless steel, and aluminum. Examples of the preferred ceramics include alumina, zirconia, silicon nitride, aluminum nitride, and other fine ceramics. Examples of the preferred resin include PET resins, PEN resins, aramid resins, polyimide resins, nylon resins, liquid crystal polymers, PEEK resins, polyimide resins, polyamide-imide resins, polyethersulfone resins, polyphenylene sulfide resins, PTFE resins, and ETFE resin. In view of preventing warping of the coreless support by heating during mount of the electronic element, these materials more preferably have a thermal expansion coefficient (CTE) of less than 25 ppm/K (typically 1.0 to 23 ppm/K). Examples of such materials include the above-mentioned resins (especially low-thermal-expansion resins such as polyimide resins and liquid crystal polymers), glass, and ceramics. In view of handling and flatness during chip mounting, the Vickers hardness of the carrier 12 is preferably 100 HV or more, more preferably 150 to 2500 HV. In terms of material satisfying these properties, the carrier 12 is preferably composed of resin, glass or ceramics, more preferably composed of glass or ceramics, most preferably composed of glass. For example, the carrier 12 is a glass sheet. The carrier 12 composed of glass has advantages such as lightweight, low thermal expansion coefficient, high insulating property, rigidity and a flat surface, so that the surface of the extremely-thin copper layer 18 can be made extremely smooth. The glass carrier has further advantages, such as high visibility contrast with copper plating at the time of image inspection after formation of the wiring layer on the surface of the coreless support, surface flatness (coplanarity) suitable for mounting an electronic device, resistance against chemicals in the desmear process of manufacturing a printed wiring board and various plating processes, and separation of the laminate with the build-up layer described later by a chemical separation process. Examples of the preferred glass constituting the carrier 12 include quartz glass, borosilicate glass, non-alkali glass, soda-lime glass, aminosilicate glass, and combinations thereof, particularly preferably non-alkali glass. The non-alkali glass is substantially free of alkali metal and mainly contains alkaline earth metal oxide, e.g., silicon dioxide, aluminum oxide, boron oxide, and an alkaline earth metal oxide, such as calcium oxide and barium oxide, and boric acid. The non-alkali glass has a low stable thermal expansion coefficient of 3 to 5 ppm/K in a wide temperature range from 0° C. to 350° C., so that warp of the glass is advantageously minimized during mount of a semiconductor chip as an electronic element. The carrier has a thickness of preferably 100 to 2000 μm, more preferably 300 to 1800 μm, most preferably 400 to 1100 μm. The carrier having a thickness within such a range can achieve thinning of the printed wiring board and a reduction in warp during mount of the electronic parts, while maintaining adequate strength that does not interfere with handling.

The surface adjacent to the interlayer 14 of the carrier 12 has an arithmetic average roughness Ra of 0.1 to 70 nm, more preferably from 0.5 to 60 nm, still more preferably from 1.0 to 50 nm, particularly preferably from 1.5 to 40 nm, most preferably from 2.0 to 30 nm, measured in accordance with JIS B 0601-2001. Thus, such a carrier having a smaller arithmetic average roughness can lead to a smaller arithmetic average roughness Ra on the surface of the extremely-thin copper layer 18 remote from the release layer 16 (the outer surface of the extremely-thin copper layer 18), resulting in a copper foil 10 provided with a carrier suitable for forming an ultrastructural wiring pattern having such a fine line/space (L/S) of (13 μm or less)/(13 μm or less) (e.g., 12 μm/12 μm to 2 μm/2 μm) in the printed wiring board.

The surface adjacent to the carrier 12 of the interlayer 14 is preferably composed of at least one metal M selected from the group consisting of Ti, Cr, Mo, Mn, W and Ni from the viewpoint of secured adhesion between the carrier 12 and the interlayer 14. The content of the metal M on the surface adjacent to the carrier 12 of the interlayer 14 is preferably 1.0 atom % or more, more preferably 3.0 atom % or more, still more preferably 4.0 atom % or more. The metal may be a pure metal or an alloy. The interlayer has no upper limit of the metal content, and thus the upper limit may be 100 atom %. The surface remote from the carrier 12 of the interlayer 14 is composed of a metal containing Cu. The surface remote from the carrier 12 (i.e., adjacent to the release layer 16) of the interlayer 14 has a Cu content of preferably 30 atom % or more, more preferably 40 atom % or more, still more preferably 50 atom % or more. The surface has no upper limit of the Cu content and thus may has a Cu content of 100 atom %.

The interlayer 14 has a thickness of preferably 5 to 1000 nm, more preferably 10 to 800 nm, still more preferably 12 to 500 nm, particularly preferably 15 to 400 nm. This thickness is determined from the cross section of the layer with transmission electron microscopy-energy dispersive X-ray spectroscopy (TEM-EDX).

The interlayer 14 may have a single layer structure as shown in FIG. 1, or may have a structure of two or more layers as shown in FIG. 2.

According to a preferred embodiment of the present invention, as shown in FIG. 2, the interlayer 14 includes an adhesive metal layer 14 a and a release assisting layer 14 b. The adhesive metal layer 14 a is disposed on the carrier 12 and is composed of at least one metal selected from the group consisting of Ti, Cr, Mo, Mn, W, and Ni. The release assisting layer 14 b is disposed on the adhesive metal layer 14 a and is composed of copper. Thus, an adhesive metal layer 14 a composed of a predetermined metal and a release assisting layer 14 b disposed in this order between the carrier 12 and the release layer 16 of the copper foil 10 provided with a carrier can provide high peeling resistance against developer in the photoresist developing process, and high stability of mechanical peel strength of the carrier. Although the mechanism by which the combination of the adhesive metal layer 14 a and the release assisting layer 14 b has the above effect is not clarified, it can be presumed as follows. Copper constituting the release assisting layer 14 b can provide stable releasability due to lower adhesion with the material (for example, carbon) constituting the release layer 16, but can provide an instable adhesion and releasability between the release assisting layer and the carrier (for example, glass or ceramics). In this respect, it is presumed that the adhesive metal layer 14 a interposed between the release assisting layer 14 b and the carrier 12 provide advantageously excellent release stability and peeling resistance against the developer between the release assisting layer 14 b and the carrier 12 and excellent wiring pattern formability by preventing the detachment of the interlayer accompanied by peeling off of the coreless support or the carrier.

The adhesive metal layer 14 a is preferably composed of at least one metal selected from the group consisting of Ti, Cr, Mo, Mn, W and Ni from the viewpoint of secured adhesion between the carrier 12 and the release assisting layer 14 b, and may be composed of a pure metal or an alloy. It is most preferred that the adhesive metal layer 14 a be composed of Ti because the adhesion of the carrier 12 to the adhesive metal layer 14 a and the release assisting layer 14 b is secured to significantly prevent peeling of the extremely-thin copper layer in the process of forming a coreless support wiring layer described later and peelings of the adhesive metal layer 14 a and the release assisting layer 14 b, which provides metal adjacent to the carrier when the coreless support is peeled, which is described later. The metal constituting the adhesive metal layer 14 a may contain incidental impurities derived from, for example, raw material components and the deposition process. In the case that the product is exposed to the atmosphere after the deposition of the adhesive metal layer 14 a, oxygen may be incorporated into the product without particular limitation. The adhesive metal layer 14 a is preferably formed by vapor phase deposition such as sputtering. The adhesive metal layer 14 a is particularly preferably formed by magnetron sputtering with a metal target in terms of improved uniformity of the film thickness distribution. The adhesive metal layer 14 a has a thickness of preferably 5 to 500 nm, more preferably 10 to 300 nm, most preferably 18 to 200 nm, particularly preferably 20 to 100 nm. This thickness is determined from the cross section of the layer with transmission electron microscopy-energy dispersive X-ray spectroscopy (TEM-EDX).

The release assisting layer 14 b is composed of copper. The copper constituting the release assisting layer 14 b may contain incidental impurities derived from, for example, raw material components and the deposition process. The release assisting layer 14 b may contain at least one metal selected from the group consisting of Si, Al, Ni, Mn, Mg, Nd, Nb, Ag, Zn, Sn, Bi, and Fe within a content not impairing the releasability of the carrier. In this case, the release assisting layer may be mainly containing copper. It is accordingly preferred that the content of the Cu element in the release assisting layer 14 b be 50 to 100 atom %, more preferably 60 to 100 atom %, still more preferably 70 to 100 atom %, particularly preferably 80 to 100 atom %, most preferably 90 to 100 atom %. In the case that the product is exposed to the atmosphere after or before the deposition of the release assisting layer 14 b, oxygen may be incorporated into the product. It is preferred, but should not be limited, that the adhesive metal layer 14 a and the release assisting layer 14 b be continuously formed without being exposed to the air. The release assisting layer 14 b is preferably formed by vapor phase deposition such as sputtering. The release assisting layer 14 b is particularly preferably formed by magnetron sputtering with a copper target in view of the improved uniformity of film thickness distribution. The release assisting layer 14 b has a thickness of preferably 5 to 500 nm, more preferably 10 to 400 nm, most preferably 15 to 300 nm, particularly preferably 20 to 200 nm. This thickness is determined from the cross section of the layer with transmission electron microscopy-energy dispersive X-ray spectroscopy (TEM-EDX).

It should be noted that another intervening layer may be present between the adhesive metal layer 14 a and the release assisting layer 14 b. Examples of constituent materials of the intervening layer include alloys of Cu with at least one metal selected from the group consisting of Ti, Cr, Mo, Mn, W and Ni.

According to another preferred embodiment of the present invention, the interlayer 14 may be an intermediate alloy layer, as shown in FIG. 1. In other words, the interlayer 14 can have a single-layer structure. The interlayer 14 as an intermediate alloy layer is preferably composed of a copper alloy containing 1.0 atom % or more at least one metal M selected from the group consisting of Ti, Cr, Mo, Mn, W and Ni and 30 atom % or more copper. In detail, it is preferred that the metal constituting the intermediate alloy layer be a copper alloy of a metal M and Cu in view of compatibility between the secured adhesion of the carrier 12 to the interlayer 14 and the ease of release to the release layer 16. Among them, an alloy of Cu and at least one metal selected from the group consisting of Ti, Mo, and Mn is more preferred. The content of the metal M in the intermediate alloy layer is preferably 1.0 atom % or more, more preferably 3.0 atom % or more, still more preferably 5.0 atom % or more. The metal M content in the intermediate alloy layer has no upper limit, but has preferably 30 atom % or less, more preferably 20 atom % or less. The intermediate alloy layer has a Cu content of preferably 30 atom % or more, more preferably 40 atom % or more, still more preferably 50 atom % or more. The intermediate alloy layer has no upper limit of the Cu content, but has a Cu content of preferably 99.5 atom % or less, more preferably 97.0 atom % or less, most preferably 96.0 atom % or less. The intermediate alloy layer is preferably formed by vapor phase deposition process such as sputtering. It is particularly preferred that the intermediate alloy layer be formed by magnetron sputtering with a copper alloy target from the viewpoint of the improved uniformity of the film thickness distribution. The intermediate alloy layer has a thickness of preferably 5 to 500 nm, more preferably 10 to 400 nm, most preferably 15 to 300 nm, particularly preferably 20 to 200 nm. This thickness is determined from the cross section of the layer with transmission electron microscopy-energy dispersive X-ray spectroscopy (TEM-EDX). Another intervening layer may be present in the intermediate alloy layer. Examples of constituent materials of the intervening layer include alloys of Cu with at least one metal selected from the group consisting of Ti, Cr, Mo, Mn, W, and Ni.

The release layer 16 facilitates the release of the carrier 12 (which is accompanied by the interlayer 14), and may be either an organic release layer or an inorganic release layer. Examples of the organic component used in the organic release layer include nitrogen-containing organic compounds, sulfur-containing organic compounds, and carboxylic acids. Examples of the nitrogen-containing organic compounds include triazole compounds and imidazole compounds. Examples of the inorganic component used in the inorganic release layer include at least one metal oxide of Ni, Mo, Co, Cr, Fe, Ti, W, P and Zn, and examples of the layer include a carbon layer. Among these, the particularly preferred release layer 16 is mainly composed of carbon, from the viewpoint of releasability and film forming property, more preferably composed of carbon or hydrocarbon, more preferably amorphous carbon, which is a hard carbon film. In this case, the release layer 16 (i.e., carbon layer) has a carbon content of preferably 60 atom % or more, more preferably 70 atom % or more, most preferably 80 atom % or more, particularly preferably 85 atom % or more, measured by XPS. The release layer has no upper limit of carbon content, and the upper limit may be 100 atom %, but realistically 98 atom % or less. The release layer 16 (especially carbon layer) may contain incidental impurities (e.g., oxygen, carbon, and hydrogen derived from the surrounding environment such as atmosphere). Furthermore, metal atoms may be incorporated into the release layer 16 (especially carbon layer) during the deposition process of the antireflective layer 17 or the extremely-thin copper layer 18. Low interdiffusion and reactivity with carriers of carbon can prevent formation of metal bond between the copper foil layer and the bonding interface caused by high temperature during press processing at a temperature exceeding 300° C., resulting in maintaining ready removal of carriers. This release layer 16 is also preferably formed by vapor phase deposition process such as sputtering in view of a reduction in excess impurities in the amorphous carbon and the continuous productivity with the deposition of the interlayer 14. The release layer 16 has a thickness of preferably 1 to 20 nm, more preferably 1 to 10 nm. This thickness is determined from the cross section of the layer with transmission electron microscopy-energy dispersive X-ray spectroscopy (TEM-EDX).

The antireflective layer 17 disposed as desired functions to prevent reflection of light. Preferably, the antireflective layer 17 is composed of at least one metal selected from the group consisting of Cr, W, Ta, Ti, Ni and Mo, and at least the surface adjacent to the extremely-thin copper layer 18 is composed of an aggregate of metal particles. In this case, the antireflective layer 17 may have a layer structure composed entirely of an aggregate of metal particles, or a layer structure of a several layers including a layer composed of aggregates of metal particles and a layer which is non-particulate at the bottom thereof. As described above, the aggregate of metal particles of the surface adjacent to the extremely-thin copper layer 18 of the antireflective layer 17 exhibits a desirable dark color due to the metal material and granular form, and its dark color provides a desirable visual contrast to the wiring layer composed of copper, resulting in the improved visibility in image inspection (e.g., automatic optical inspection (AOI)). That is, the surface of the antireflective layer 17 diffusely reflects light due to the convex shape of the metal particles to be visually recognized as black. Furthermore, the antireflective layer 17 has an adequate adhesion and releasability with respect to the release layer 16, excellent adhesion to the extremely-thin copper layer 18, and high peeling resistance against the developer at the time of forming the photoresist layer. The glossiness Gs (60°) of the surface of the antireflective layer 17 adjacent to the extremely-thin copper layer 18 is preferably 500 or less in view of such improved contrast and visibility, more preferably 450 or less, still more preferably 400 or less, particularly preferably 350 or less, and most preferably 300 or less. The lower limit of the glossiness Gs (60°) is preferably as low as possible, but the surface adjacent to the extremely-thin copper layer 18 of the antireflective layer 17 has a glossiness Gs (60°) of effectively 100 or more, and more effectively 150 or more. The specular glossiness Gs (60°) is determined by image analysis of roughened particles in accordance with JIS Z 8741-1997 (specular glossiness—measurement method) with a commercially available gloss meter.

In more detail, a copper foil provided with a carrier in which an antireflective layer 17 composed of a predetermined metal, having an aggregate of metal particles at least on the surface adjacent to the extremely-thin copper layer 18, is interposed between the release layer 16 and the extremely-thin copper layer 18 has the following advantages: (1) excellent chemical resistance of the antireflective layer against the copper flash etching solution during the formation of the wiring layer on the surface of the coreless support and (2) excellent visibility of the wiring layer due to high contrast to the antireflective layer in image inspection (e.g., automatic optical inspection (AOI)) after copper flash etching. Regarding advantage (1), at least one metal selected from Cr, W, Ta, Ti, Ni and Mo constituting the antireflective layer 17 cannot be etched away in the copper flash etching solution, and thus exhibits high chemical resistance against the copper flash etching solution. Regarding advantage (2), the aggregate of metal particles constituting at least the surface adjacent to the extremely-thin copper layer 18 of the antireflective layer 17 exhibits a desirable dark color due to the metallic material and granular form, and its dark color provides a desirable visual contrast to the wiring layer composed of copper, resulting in the improved visibility in image inspection (e.g., automatic optical inspection (AOI)). In addition, the manufacture of a coreless support provided with a wiring layer or a printed wiring board using the copper foil provided with a carrier of the present invention has further advantage (3): The erosion of the wiring layer exposed under the antireflective layer can be significantly reduced when the antireflective layer is removed by flash etching. In other words, a highly selective etching solution may be used in flash etching at least one metal selected from Cr, W, Ta, Ti, Ni and Mo constituting the antireflective layer 17 to reduce or prevent etching away of the copper from the wiring layer in the etching solution.

In view of improved contrast and visibility and improved uniformity of flash etching, the surface adjacent to the extremely-thin copper layer 18 of the antireflective layer 17 is preferably composed of an aggregate of metal particles having a projected area circle equivalent diameter of preferably 10 to 100 nm, more preferably 25 to 100 nm, and most preferably 65 to 95 nm, determined by SEM image analysis. Such a projected area circle equivalent diameter can be determined by photographing the surface of the antireflective layer 17 with a scanning electron microscope at a predetermined magnification (e.g., 50,000 times) and analyzing the observed SEM image. Specifically, the arithmetic mean value of projected area circle equivalent diameters measured using commercially available image analysis particle size distribution software is preferably employed.

The antireflective layer 17 is composed of at least one metal selected from Cr, W, Ta, Ti, Ni and Mo, preferably at least one metal selected from Ta, Ti, Ni and Mo, more preferably at least one metal selected from Ti, Ni and Mo, most preferably Ti. These metals may be either pure metals or alloys. In any event, essentially unoxidized metals (essentially not metal oxides) are preferred because they exhibit a desired dark color which improves the visual contrast to Cu. Specifically, the antireflective layer 17 has an oxygen content of preferably 0 to 15 atom %, more preferably 0 to 13 atom %, most preferably 1 to 10 atom %. In any case, the metal cannot be etched away in the copper flash etching solution, and thus exhibits high chemical resistance against the copper flash etching solution. The antireflective layer 17 has a thickness of preferably 1 to 500 nm, more preferably 10 to 300 nm, most preferably 20 to 200 nm, particularly preferably 30 to 150 nm.

The extremely-thin copper layer 18 may be manufactured by any process. Examples of the process include wet processes, such as electroless copper plating and electrolytic copper plating; physical vapor deposition, such as sputtering and vacuum vapor deposition; chemical vapor deposition; and combination thereof. A particularly preferred extremely-thin copper layer is manufactured by vapor phase deposition, for example, sputtering or vacuum vapor deposition because the resulting copper foil is extremely-thin and is suitable to meet a fine pitch, and the most preferred is manufactured by sputtering. Although the extremely-thin copper layer is preferably not roughened, the layer may be preliminarily or secondarily roughened by soft etching, rinsing, or oxidation-reduction with proviso that the wiring pattern can be readily formed during the production of printed wiring boards. Although the extremely-thin copper layer 18 may have any thickness, the layer has a thickness of preferably 50 to 3000 nm, more preferably 70 to 2500 nm, still more preferably 80 to 2000 nm, particularly preferably 90 to 1500 nm, most preferably 120 to 1000 nm or 150 to 500 nm to satisfy the fine pitch as described above. The extremely-thin copper layer having such a thickness within this range is preferably manufactured by sputtering from the viewpoint of uniformity of in-plane thickness of layer and productivity in sheet form or roll form.

The extremely-thin copper layer 18 has a surface remote from the release layer 16 (the outer surface of the extremely-thin copper layer 18), and the surface has an arithmetic average roughness Ra of preferably 1.0 to 100 nm, more preferably from 2.0 to 40 nm, still more preferably from 3.0 to 35 nm, particularly preferably from 4.0 to 30 nm, most preferably from 5.0 to 15 nm, measured in accordance with JIS B 0601-2001. Such a copper foil 10 provided with a carrier having a smaller arithmetic average roughness is suitable for forming an ultrastructural wiring patter having such a fine line/space (US) of (13 μm or less)/(13 μm or less) (e.g., 12 μm/12 μm to 2 μm/2 μm) in the printed circuit board.

It is preferred that the extremely-thin copper layer 18, the optional antireflective layer 17, the optional interlayer 14 (e.g., the adhesive metal layer 14 a and/or the release assisting layer 14 b or the intermediate alloy layer), and the optional release layer 16 (i.e., at least the extremely-thin copper layer 18, for example, the extremely-thin copper layer 18 and the antireflective layer 17) extend to the end faces of the carrier 12 to cover the end faces of the carrier 12. More specifically, it is preferred that not only the surface but also the end faces of the carrier 12 be covered with at least the extremely-thin copper layer 18. Covering the end faces in addition to the surface can prevent intrusion of the chemical solution from the carrier 12 in the printed wiring board process, and also can effectively prevent chipping due to peeling at the side ends, i.e., chipping of the coating on the release layer 16 (i.e., the extremely-thin copper layer 18 and the antireflective layer 17, if present) when the coreless support is handled (for example, when the coreless support is carried by rollers). The adhesive metal layer 14 a has a thickness (in the direction perpendicular to the end face, hereinafter referred to as “end-face thickness”) on the end face of the carrier 12 of preferably 2 to 350 nm, more preferably 3 to 220 nm, most preferably 5 to 150 nm, particularly preferably 6 to 70 nm. The release assisting layer 14 b has an end-face thickness of preferably 2 to 350 nm, more preferably 3 to 220 nm, most preferably 5 to 150 nm, particularly preferably 6 to 70 nm. The interlayer 14 as an intermediate alloy layer has an end-face thickness of preferably 2 to 350 nm, more preferably 3 to 220 nm, most preferably 5 to 150 nm, particularly preferably 6 to 70 nm. The release layer 16 has an end-face thickness of preferably 0 to 15 nm, more preferably 0 to 3 nm, most preferably 0 to 1 nm, particularly preferably 0 to 0.5 nm, most preferably 0 nm. In other words, it is most preferred that the release layer 16 be not formed on the end faces of the carrier. The antireflective layer 17 has an end-face thickness of preferably 2 to 350 nm, more preferably 3 to 220 nm, most preferably 5 to 150 nm, particularly preferably 6 to 70 nm. The extremely-thin copper layer 18 has an end-face thickness of preferably 15 to 2800 nm, more preferably 20 to 1800 nm, most preferably 25 to 1400 nm, particularly preferably 27 to 1350 nm, particularly preferably 35 to 700 nm, most preferably 45 to 350 nm. Furthermore, the coating region on the end faces of the carrier 12 covers a region of preferably 0.1 mm or more in the thickness direction (perpendicular to the carrier surface) from the surface of the carrier 12, more preferably a region of 0.2 mm or more, more preferably the entire end face of the carrier 12. In this way, chipping of the film at the side ends of the coreless support and the penetration of the chemical liquid into the carrier in the printed wiring board process can be effectively prevented.

Production of Copper Foil Provided with Carrier

It is preferred that the copper foil 10 provided with a carrier of the present invention can be manufactured by providing the carrier 12 and forming an interlayer layer 14 (e.g., double-layer structure of an adhesive metal layer 14 a and a release assisting layer 14 b or one layer structure of an intermediate alloy layer), a release layer 16, an optional antireflective layer 17 (if present), and a extremely-thin copper layer 18 be formed by vapor phase deposition because they are suitable for fine pitch requirements due to extremely-thin standards. Examples of the vapor phase deposition include sputtering, vacuum vapor deposition, and ion plating, most preferably sputtering from the viewpoint of controlling the film thickness over a wide range of 0.05 nm to 5,000 nm and maintaining the uniform film thickness over a wide width or wide area. In particular, forming all of the interlayer 14, the release layer 16, the antireflective layer 17 (if present), and the extremely-thin copper layer 18 by sputtering remarkably enhances the efficiency of manufacturing. The vapor phase deposition process can be carried out under known conditions with any known vapor deposition system. For example, if sputtering is used, then any of various known sputtering techniques such as magnetron sputtering, bipolar sputtering and counter target sputtering can be used. Magnetron sputtering is preferred in view of high deposition rate and high productivity. Sputtering can be performed with a direct current (DC) supply or radio frequency (RF) supply. Regarding the target shape, a well-known plate target can be used, but it is desirable to use a cylindrical target from the viewpoint of the efficiency of use of the target. Vapor phase deposition of each of the interlayer 14 (e.g., double-layer structure of an adhesive metal layer 14 a and a release assisting layer 14 b or one layer structure of an intermediate alloy layer), the release layer 16, the antireflective layer 17 (if present), and the extremely-thin copper layer 18 (preferably a sputtering) will be described.

It is preferred that vapor phase deposition of the adhesive metal layer 14 a be carried out by magnetron sputtering in a non-oxidizing atmosphere with a target composed of at least one metal selected from the group consisting of Ti, Cr, and Ni in view of improved uniformity in film thickness distribution. The silicon target preferably has a purity of 99.9% or more. The gas used for sputtering includes inert gas such as argon gas. Argon can be supplied at any flow rate, which may be determined as appropriate according to dimensions of the sputtering chamber and deposition conditions. The pressure during film deposition is preferably set in a range of 0.1 to 20 Pa from the view point of continuous formation of a stable film without operation failures such as abnormal discharge and plasma irradiation failure. This pressure range can be set by adjusting the electric power for film deposition and the flow rate of argon depending on the structure and volume of the device, the exhaust capacity of the vacuum pump, and the rated capacity of power supply for the film deposition. The sputtering power (per unit area of the target) can be appropriately determined within the range of 0.05 to 10.0 W/cm² from the view point of, for example, the uniform thickness and productivity of the film.

It is preferred that vapor phase deposition of the release assisting layer 14 b be carried out by magnetron sputtering with a copper target under a non-oxidizing atmosphere in terms of the uniformity in film thickness distribution. The copper target preferably has a purity of 99.9% or more. The gas used for sputtering is preferably inert gas such as argon gas. Argon can be supplied at any flow rate, which may be determined as appropriate according to dimensions of the sputtering chamber and deposition conditions. The pressure during film deposition is preferably set in a range of 0.1 to 20 Pa from the view point of continuous formation of a stable film without operation failures such as abnormal discharge and plasma irradiation failure. This pressure range can be set by adjusting the electric power for film deposition and the flow rate of argon depending on the structure and volume of the device, the exhaust capacity of the vacuum pump, and the rated capacity of power supply for the film deposition. The sputtering power (per unit area of the target) can be appropriately determined within the range of 0.05 to 10.0 W/cm² from the view point of, for example, the uniform thickness and productivity of the film.

It is preferred that the interlayer 14 of the intermediate alloy layer be deposited by magnetron sputtering with an alloy target of Cu with at least one metal M selected from the group consisting of Ti, Cr, Mo, Mn, W and Ni under a non-oxidizing atmosphere in terms of the uniformity in film thickness distribution. The copper target preferably has a purity of 99.9% or more. The gas used for sputtering is preferably inert gas such as argon gas. Argon can be supplied at any flow rate, which may be determined as appropriate according to dimensions of the sputtering chamber and deposition conditions. The pressure during film deposition is preferably set in a range of 0.1 to 20 Pa from the view point of continuous formation of a stable film without operation failures such as abnormal discharge and plasma irradiation failure. This pressure range can be set by adjusting the electric power for film deposition and the flow rate of argon depending on the structure and volume of the device, the exhaust capacity of the vacuum pump, and the rated capacity of power supply for the film deposition. The sputtering power (per unit area of the target) can be appropriately determined within the range of 0.05 to 10.0 W/cm² from the view point of, for example, the uniform thickness and productivity of the film.

It is preferred that the release layer 16 be deposited by a vapor phase deposition (preferably sputtering) with a carbon target under an inert atmosphere such as argon. The carbon target is preferably composed of graphite, but may contain incidental impurities (e.g., oxygen or carbon from the surrounding environment such as atmosphere). The carbon target preferably has a purity of 99.99% or more, more preferably 99.999% or more. Furthermore, the pressure during film deposition is preferably set in a range of 0.1 to 2.0 Pa from the view point of continuous formation of a stable film without operation failures such as abnormal discharge and plasma irradiation failure. This pressure range can be set by adjusting the electric power for film deposition and the flow rate of argon depending on the structure and volume of the device, the exhaust capacity of the vacuum pump, and the rated capacity of power supply for the film deposition. The sputtering power (per unit area of the target) can be appropriately determined within the range of 0.05 to 10.0 W/cm² from the view point of, for example, the uniform thickness and productivity of the film.

It is preferred that the antireflective layer 17 be deposited by magnetron sputtering with a metal target composed of at least one metal selected from the group consisting of Cr, W, Ta, Ti, Ni, and Mo. The target has preferably a purity of 99.9% or more. In particular, the antireflective layer 17 is preferably formed by a magnetron sputtering in an inert gas atmosphere such as argon at a pressure of 1 to 20 Pa. The sputtering pressure is more preferably 2 to 18 Pa, still more preferably 3 to 15 Pa. Such a sputtering pressure is remarkably higher than conventional sputtering pressures, so that an aggregate of metal particles can be formed in a desired form uniformly in the in-plane surface without essentially oxidizing the surface of the antireflective layer 17. The above sputtering conditions can provide a desired projected area circle equivalent diameter and a desired glossiness Gs (60°) and can also advantageously provide continuous formation of a stable film without operation failures such as abnormal discharge and plasma irradiation failure. The pressure range may be controlled by adjusting the electric power for film deposition and the flow rate of the argon gas depending on the structure and volume of the device, the exhaust capacity of the vacuum pump, and the rated capacity of power supply for the film deposition. Argon can be supplied at any flow rate, which may be determined as appropriate according to dimensions of the sputtering chamber and deposition conditions. The sputtering power (per unit area of the target) can be appropriately determined within the range of 1.0 to 15.0 W/cm² from the view point of, for example, the uniform thickness and productivity of the film. Furthermore, it is preferred that the carrier temperature be kept constant during film formation in view of ease of achieving stable film characteristics (for example, film resistance and crystal size). The carrier temperature during film formation is preferably adjusted within the range of 25 to 300° C., more preferably 40 to 200° C., and furthermore preferably 50 to 150° C.

The extremely-thin copper layer 18 is preferably formed by vapor phase deposition (preferably sputtering process) under an inert atmosphere such as argon with a copper target. The copper target is preferably composed of metallic copper, but may contain incidental impurities. The carbon target preferably has a purity of 99.9% or more, more preferably 99.99% or more, still more preferably 99.999%. A cooling mechanism for the stage may be provided at the time of sputtering to avoid a temperature rise during the vapor phase deposition of the extremely-thin copper layer 18. The pressure during film deposition is preferably set in a range of 0.1 to 2.0 Pa from the view point of continuous formation of a stable film without operation failures such as abnormal discharge and plasma irradiation failure. This pressure range can be set by adjusting the electric power for film deposition and the flow rate of argon depending on the structure and volume of the device, the exhaust capacity of the vacuum pump, and the rated capacity of power supply for the film deposition. The sputtering power (per unit area of the target) can be appropriately determined within the range of 0.05 to 10.0 W/cm² from the view point of, for example, the uniform thickness and productivity of the film.

The interlayer 14, the release layer 16, the antireflective layer 17 and/or the extremely-thin copper layer 18 on the end faces of the carrier 12 can be readily formed by deposition while the end face of the carrier 12 is being exposed on the stage in the sputtering process. In this case, the end face of the carrier 12 is typically formed into a thickness (end-face thickness) of 20% to 70% of the thickness of the layer deposited on the surface of the carrier 12. In the meantime, in the case of forming an extremely-thin film on the end face, such as forming the release layer 16, it is preferred to sputter with the side ends of the carrier 12 shielded. Examples of this type of shielding include shielding by a masking tape and shielding by a masking plate.

Laminate for Coreless Support

The copper foil provided with a carrier of the present invention may be provided in the form of a laminate for a coreless support. In other words, a preferred embodiment of the present invention provides a laminate for a coreless support comprising the copper foil provided with a carrier. The laminate for a coreless support has the following two forms: (i) The first form of the laminate for a coreless support is in the form of the copper foil 10 provided with a carrier itself. In detail, the interlayer 14, the release layer 16, the optional antireflective layer 17, and the extremely-thin copper layer 18 are formed in this order on at least one surface of the carrier 12; or the interlayer 14, the release layer 16, the optional antireflective layer 17, the extremely-thin copper layer 18 are formed in this order on each surface of the carrier. In any case, this form can be achieved if the carrier 12 itself is rigid such as a glass plate or a metal plate and can function as a support. For example, a glass carrier 12, which is lightweight, has a low thermal expansion coefficient, is rigid and has a flat surface, has an advantage in that the surface of the extremely-thin copper layer 18 can be extremely smooth. (ii) The second form of the laminate for a coreless support may be provided in a form having an adhesive layer on the outer surface of the carrier 12 (the outer surface of the carrier 12 being remote from the release layer 16). This form is available in the case where the carrier 12 is composed of a nonrigid material such as a metal foil or a resin film. In this case, examples of the adhesive layer include a resin layer and a fiber reinforced prepreg (such as glass). For example, a possible layer configuration consists of an extremely-thin copper layer 18, an optional antireflective layer 17, a release layer 16, an interlayer 14, a carrier 12, an adhesive layer (not shown), a carrier 12, an interlayer 14, a release layer 16, an optional antireflective layer 17, and an extremely-thin copper layer 18. The interlayer 14 may has a double layer structure of an adhesive metal layer 14 a and a release assisting layer 14 b in this order from the carrier 12 side, or may be a single intermediate alloy layer as described above.

Production of Coreless Support Provided with Wiring Layer

A coreless support provided with a wiring layer can be manufactured using a copper foil provided with a carrier of the present invention. Hereinafter, a preferred method of manufacturing a coreless support provided with a wiring layer will be described. The method of manufacturing a coreless support provided with a wiring layer includes steps of: (1) preparing a copper foil provided with a carrier, (2) forming a photoresist layer, (3) forming an electrolytic copper plating layer, (4) peeling off the photoresist layer, and (5) flash etching. The production of a coreless support provided with a wiring layer including these steps is schematically shown in FIGS. 3 and 4.

(1) Preparation of Copper Foil Provided with Carrier.

A support for the copper foil 10 provided with a carrier is provided (see FIG. 3(a)). As described above, the copper foil 10 provided with a carrier can be provided in the form of a laminate for a coreless support. In other words, as described above, the copper foil provided with a carrier may be provided in a form of a carrier foil itself, or may be provided in a form having an adhesive layer on the outer surface of the carrier 12 (the outer surface of the carrier 12 being remote from the release layer 16), for example, in a form of a layer structure consisting of an extremely-thin copper layer 18, an optional antireflective layer 17, a release layer 16, an interlayer 14, a carrier 12, an adhesive layer (not shown), a carrier 12, an interlayer 14, a release layer 16, an optional antireflective layer 17, and an extremely-thin copper layer 18. The interlayer 14 may has a double layer structure consisting of an adhesive metal layer 14 a and a release assisting layer 14 b in order from the carrier 12 side as shown in FIGS. 3 and 4, or may has a single layer structure consisting of an intermediate alloy layer shown in FIG. 1.

(2) Formation of Photoresist Layer

A photoresist layer 20 is formed in a predetermined pattern on the surface of the extremely-thin copper layer 18 (see FIG. 3(b)). The photoresist is preferably a photosensitive film, for example, a photosensitive dry film. The photoresist layer 20 may be provided with a predetermined wiring pattern by exposure and development. In this case, the copper foil 10 provide with a carrier of the present invention, which has the interlayer 14, can exhibit high peeling resistance against a developer (for example, aqueous sodium carbonate solution).

(3) Formation of Electrolytic Copper Plating Layer

An electrolytic copper plating layer 22 is formed on the exposed surface of the extremely-thin copper layer 18 (i.e., the portion not masked with the photoresist layer 20) (see FIG. 3(c)). The electrolytic copper plating can be carried out by any known process without any limitation.

(4) Peeling-Off of Photoresist Layer

The photoresist layer 20 is then peeled off. As shown in FIG. 4(d), the electrolytic copper plating layer 22 remains in the form of a wiring pattern, and the portions of extremely-thin copper layer 18 where the wiring pattern is not formed are exposed.

(5) Copper Flash Etching

Unnecessary portions of the extremely-thin copper layer 18 are removed by copper flash etching to prepare a coreless support (hereinafter referred to as a coreless support 26 provided with a wiring layer) on which the wiring layer 24 is formed. In the case where the copper foil 10 with a carrier has the antireflective layer 17, the unnecessary portions of the extremely-thin copper layer 18 are removed by copper flash etching to leave the antireflective layer 17 exposed (that is, the copper flash etching is stopped on the antireflective layer 17). It is preferred that the flashing liquid contain at least one of a mixture of sulfuric acid and hydrogen peroxide, sodium persulfate and potassium persulfate because the exposed extremely-thin copper layer 18 can be reliably etched while excess etching of the electrolytic copper plating layer 22 is prevented. Thus, as shown in FIG. 4(e), the electrolytic copper plating layer 22 and the extremely-thin copper layer 18 remain in the form of a wiring pattern, while portions of the antireflective layer 17 where the wiring pattern is not formed are not eluted by the flash etching solution to be exposed on the surface. At least one metal selected from Cr, W, Ta, Ti, Ni, and Mo constituting the antireflective layer 17 cannot be eluted in the copper flash etching solution, and thus exhibits high chemical resistance against the copper flash etching solution. In other words, the antireflective layer 17 is not removed during copper flash etching but is left in the exposed state for the next image inspection process.

(6) Image Inspection and Other Steps (Optional Process)

After the copper flash etching, it is preferred that the image of the coreless support 26 provided with a wiring layer (specifically, the wiring layer 24) be inspected. Typically, the image is inspected as follows: a binary image of a wiring pattern is acquired with an automatic optical inspection (AOI) system by irradiating the support with predetermined light from a light source. Pattern matching between the binary image and the design data image is then carried out to evaluate match or mismatch between these images. It is preferred that the image inspection be performed while the antireflective layer 17 (if present) remains exposed. The aggregate of metal particles constituting at least the surface of the antireflective layer 17 exhibits a desirable dark color due to the metallic material and granular form, leading to a desirable visual contrast to the wiring layer 24 composed of copper, resulting in improved visibility in image inspection (e.g., automatic optical inspection (AOI)).

After the above image inspection, it is preferred to mount an electronic element 28, such as a chip, on the coreless support 26 provided with wiring layer, if necessary. A printed wiring board can thereby be manufactured. As described above, such a process of mounting the chip after forming the wiring layer 24 is called RDL-first process. This method enables image inspection of the wiring layer on the surface of the coreless support and each build-up wiring layer stacked thereafter, prior to chip mounting, so that the chip may be mounted only on the non-defective portion of each wiring layer. As a result, the RDL-first method, which can avoid wasteful use of the chips, is economically advantageous compared to the Chip-first method, which sequentially stacks the wiring layer on the surface of the chip. In the case where the copper foil 10 with a carrier of the present invention has the antireflective layer 17, there is provided sufficient contrast between the surface of the electrolytic copper plating layer 22 and the surface of the antireflective layer 17 in image inspection, resulting in high-accuracy image inspection. Accordingly, for example, the binary images of the wiring pattern acquired by the automatic optical inspection (AOI) system are more accurate and clear. Thus, in the process of manufacturing a printed wiring board (in particular, the RDL-first process), images on a wiring layer before chip mounting can be inspected with high accuracy, resulting in improved product yield. Examples of the optional electronic element 28 mounted on the wiring layer of the coreless support 26 include a semiconductor element, a chip capacitor, and a resistor. Examples of a method of mounting electronic elements include a flip chip mounting method and a die bonding method. The flip chip mounting method involves bonding the mounting pad of the electronic elements 28 to the wiring layer 24 on the coreless support 26. Columnar electrodes (pillars) and solder bumps a may be formed on this mounting pad. A sealing resin film such as non-conductive film (NCF) may be attached to the surface of the wiring layer 24 of the coreless support 26 before mounting. Although the bonding is preferably performed using a low melting point metal such as solder, an anisotropic conductive film may be used. In the die bonding method, the surface opposite to the mounting pad surface of the electronic element 28 is bonded to the wiring layer 24 on the surface of the coreless support 26. For this bonding, it is preferred to use a paste or a film composed of a resin composition containing a thermosetting resin and a thermally conductive inorganic filler.

Production of Printed Wiring Board

The printed wiring board can be manufactured using the coreless support provided with the wiring layer of the present invention. Hereinafter, a preferred manufacturing method of the printed wiring board will be described. The method of manufacturing this printed wiring board involves the steps of (1) manufacturing a coreless support provided with a wiring layer, (2) preparing a laminate with a build-up layer, (3) separating the laminate with a build-up layer, and (4) processing a multilayer wiring board. The method of manufacturing a printed wiring board including these steps is schematically shown in FIGS. 3 to 5(in particular, FIG. 5).

(1) Step of Manufacturing Coreless Support Provided with Wiring Layer

The coreless support 26 provided with wiring layer is manufactured by the method of the present invention described above. In other worlds, the production of the printed wiring board of the present invention includes a series of steps of the above-described method of manufacturing a coreless support provided with a wiring layer, and the repetitive description thereof will be omitted.

(2) Step of Preparing Laminate with Build-Up Layer

The build-up layer 30 is formed on the surface of the coreless support 26 provided with wiring layer on which the wiring layer 24 is formed to prepare a laminate 32 with a build-up layer (see FIG. 5(g)). Although details of the build-up layer 30 are not shown in FIG. 5, any known build-up wiring layer structure commonly used in printed wiring boards may be adopted.

(3) Step of Separating Laminate with Build-Up Layer

The multilayer wiring board 34 including the build-up layer 30 is prepared by separating the laminate 32 with build-up layer with the release layer 16. That is, the carrier 12, the interlayer 14, and the release layer 16 are peeled off. The separation step such as physical separation and chemical separation can be employed in the separation step. Physical separation is preferred. The physical separation involves separating the carrier 12 from the build-up layer 30 into the multilayer wiring board 34 (see FIG. 5(h)) by hand, or with a tool or a machine. In this case, the copper foil 10 with a carrier of the present invention has an interlayer 14, which leads to high stability of mechanical peel strength of the carrier 12. As a result, the carrier 12 can be readily peeled off together with the interlayer 14 and the peeling layer 16.

(4) Step of Processing Multilayer Wiring Board

The multilayer wiring board 34 is processed to prepare a printed wiring board 36 (FIG. 5(i)). In the case where the antireflective layer 17 is present in the multilayer wiring board 34, it is preferred that the antireflective layer 17 be removed by flash etching. The appropriate etching solution for the flash etching is preferably selected according to the metal constituting the antireflective layer 17, for example, as exemplified in the Table 1 below. Representative etching solutions are exemplified in Table 1, but the present invention is not limited thereto, and the conditions such as the type and concentration of acid and ammonium salt, and temperature can be appropriately varied from the conditions shown in Table 1.

TABLE 1 Constituent element of Desirable antireflective Desirable components contained in etching etching layer solution temperature Cr HNO₃ (5%) and cerium(IV) ammonium 40° C. hexanitrate (CAN)(20%) W H₂O₂ (30%), triammonium citrate (5%) and 30° C. NH₃ (0.1%) Ta NaOH (30%) 70 to 80° C. Ti H₂O₂ (30%), triammonium citrate (5%) and 30° C. NH₃ (0.1%) Ni HNO₃ (20%) and H₂O₂ (10%) 40° C. Mo H₃PO₄, HNO₃ and CH₃COOH 23° C.

The antireflective layer 17 can be selectively flash-etched with such an etching solution, so that erosion of the wiring layer 24 (which is composed of copper) exposed under the antireflective layer 17 can be significantly prevented. In other words, a highly selective etching solution may be used in flash etching of at least one metal selected from Cr, W, Ta, Ti, Ni and Mo constituting the antireflective layer 17 to reduce or prevent etching away of the copper from the wiring layer 24 in the etching solution.

The outer layer of the printed wiring board 36 as shown in FIG. 5 can be processed by various methods. For example, an insulating layer and a wiring layer as build-up wiring layers may be stacked on the wiring layer 24 of the printed wiring board 36 as any number of layers, or a solder resist layer may be formed on the surface of the wiring layer 24 to perform surface treatment as an outer layer pad such as Ni—Au plating or OSP treatment (water soluble preflux treatment, Organic Solderability Preservative). Furthermore, a columnar pillar and other features may be provided on the outer layer pad. In any case, in general, any known method employed in a printed wiring board can be additionally carried out.

EXAMPLES

The present invention will be described in further detail by way of the following examples.

Example 1

(1) Preparation of Copper Foil Provided with Carrier

As shown in FIG. 1, an adhesive metal layer 14 a, release assisting layer 14 b, a release layer 16, and an extremely-thin copper layer 18 were deposited in this order on a glass sheet carrier 12 to prepare a copper foil 10 provided with a carrier. The detailed procedures are as follows. The arithmetic average roughness Ra in the following examples is measured with a non-contact profilometer (NewView 5032 manufactured by Zygo Corporation) in accordance with JIS B 0601-2001.

(1a) Provision of Carrier

A glass sheet (material: non-alkali glass, product name: OA 10, manufactured by Nippon Electric Glass Co., Ltd.) having a thickness of 700 μm and a surface with an arithmetic average roughness Ra of 0.5 nm was provided.

The end faces of the carrier 12 were masked with a stainless steel plate, and various layers were formed by sputtering as described below.

(1b) Formation of Adhesive Metal Layer

A titanium adhesive metal layer 14 a having a thickness of 100 nm was deposited on the surface of the carrier 12 by sputtering under the following conditions:

-   -   Apparatus: single-wafer type magnetron sputtering system         (manufactured by Tokki Corporation)     -   Target: Ti target (purity: 99.999%) with a diameter of 8 inches         (203.2 mm)     -   Ultimate vacuum Pu: less than 1×10⁻⁴ Pa     -   Carrier gas: Ar (flow rate: 100 sccm)     -   Sputtering pressure: 0.35 Pa     -   Sputtering power: 2,000 W (6.2 W/cm²)     -   Temperature during deposition: 40° C.

(1c) Formation of Release Assisting Layer

A copper release assisting layer 14 b having a thickness of 100 nm was deposited on the adhesive metal layer 14 a by sputtering under the following conditions:

-   -   Apparatus: single wafer type DC sputtering system (MLS 464         manufactured by Canon Tokki Corporation)     -   Target: Cu target (purity: 99.98%) with a diameter of 8 inches         (203.2 mm)     -   Ultimate vacuum Pu: less than 1×10⁻⁴ Pa     -   Carrier gas: Ar (flow rate: 100 sccm)     -   Sputtering pressure: 0.35 Pa     -   Sputtering power: 2,000 W (6.2 W/cm²)     -   Temperature during deposition: 40° C.

(1d) Formation of Release Layer

An amorphous carbon layer having a thickness of 3 nm as a release layer 16 was deposited on the release assisting layer 14 b by sputtering under the following conditions:

-   -   Apparatus: single wafer type DC sputtering system (MLS 464         manufactured by Canon Tokki Corporation)     -   Target: carbon target (purity: 99.999%) with a diameter of 8         inches (203.2 mm)     -   Ultimate vacuum Pu: less than 1×10⁻⁴ Pa     -   Carrier gas: Ar (flow rate: 100 sccm)     -   Sputtering pressure: 0.35 Pa     -   Sputtering power: 100 W (0.3 W/cm²)     -   Temperature during deposition: 40° C.

(1e) Formation of Antireflective Layer

A nickel antireflective layer 17 having a thickness of 100 nm was deposited on the surface of the release layer 16 by sputtering under the following conditions:

-   -   Apparatus: single wafer type DC sputtering system (MLS 464         manufactured by Canon Tokki Corporation)     -   Target: Ti target (purity: 99.999%) with a diameter of 8 inches         (203.2 mm)     -   Carrier gas: Ar (flow rate: 100 sccm)     -   Ultimate vacuum Pu: less than 1×10⁻⁴ Pa     -   Sputtering pressure: 12 Pa     -   Sputtering power: 2,000 W (6.2 W/cm²)

(1f) Formation of Extremely-Thin Copper Layer

An extremely-thin copper layer 18 having a thickness of 300 nm was deposited on the antireflective layer 17 under the following conditions. The surface remote from the release layer 16 (i.e., the outer surface) of the resulting extremely-thin copper layer 18 had an arithmetic average roughness Ra of 3 nm.

-   -   Apparatus: single wafer type DC sputtering system (MLS 464         manufactured by Canon Tokki Corporation)     -   Target: Cu target (purity: 99.98%) with a diameter of 8 inches         (203.2 mm)     -   Ultimate vacuum Pu: less than 1×10−4 Pa     -   Carrier gas: Ar (flow rate: 100 sccm)     -   Sputtering pressure: 0.35 Pa     -   Sputtering power: 2,000 W (6.2 W/cm²)     -   Temperature during deposition: 40° C.

(1g) Components Analysis

The samples for, for example, components analysis are prepared under the same conditions as those of manufacturing the adhesive metal layer 14 a, release assisting layer 14 b, release layer 16, and antireflective layer 17 of the resulting copper foil provided with carrier: that is, a first sample provided with only an adhesive metal layer 14 a on a glass sheet, a second sample provided with only a release assisting layer 14 b on a glass sheet, a third sample provided with only a release layer 16 on a glass sheet, and a fourth sample provided with only an antireflective layer 17 on a glass sheet were separately prepared. Components of each sample were analyzed as follows to determine the components of each layer.

<Components Analyses of Adhesive Metal Layer, Release Assisting Layer, and Antireflective Layer>

Monitoring samples for surface analysis were prepared for the adhesive metal layer 14 a, the release assisting layer 14 b, and the antireflective layer 17 to perform elemental analysis by time-of-flight secondary ion mass spectrometry (TOF-SIMS). This measurement was carried out in a constant current mode under the condition of 800 V and 3 mA. The results of the compositions of the adhesive metal layer 14 a, the release assisting layer 14 b and the antireflective layer 17 were as follows.

Adhesive metal layer 14 a: 92.5 atom % Ti, 7.5 atom % O

Release assisting layer 14 b: 99 atom % Cu, 1 atom % O

Anti-reflective layer 17: 99.6 atom % Ti, 0.4 atom % O

<Components Analysis of Release Layer>

Elemental analysis was performed on the release layer 16 (i.e., the carbon layer) by XPS to determine the carbon content. The release layer 16 had a carbon content of 93 atom % (C+O=100%).

<Measurement of Projected Area Circle Equivalent Diameter of Antireflective Layer Surface>

The sample immediately after the formation of the antireflective layer 17 was taken out, and the surface of the antireflective layer 17 was photographed at a magnification of 50,000 with a scanning electron microscope to acquire an SEM image. The projected area circle equivalent diameters were measured by analysis of the binary image from the acquired SEM image. The image analysis was performed with image analysis type particle size distribution software (Mac-VIEW, manufactured by Mountech Co., Ltd.). For arbitrary 50 or more particles, the projected area circle equivalent diameter was measured for individual particles to calculate the arithmetic mean value thereof. The resulting projected area circle equivalent diameter of the surface of the antireflective layer 17 was 60 nm.

Example 2

A copper foil provided with a carrier was prepared and evaluated as in Example 1 except that a nickel sputtering target (purity: 99.999%) was used to form a nickel layer instead of a titanium layer as the adhesive metal layer 14 a. The results are shown in Table 2. The arithmetic average roughness Ra of the surface remote from the release layer 16 of the extremely-thin copper layer 18 was 3.7 nm. The composition of each layer other than the adhesive metal layer 14 a was substantially the same as that in Example 1. The adhesive metal layer 14 a has a composition of 99.5 atom % Ni and 0.5 atom % O.

Example 3

A copper foil provided with a carrier was prepared and evaluated as in Example 1 except that a chromium sputtering target (purity: 99.999%) was used to form a chromium layer instead of a titanium layer as the adhesive metal layer 14 a. The results are shown in Table 2. The arithmetic average roughness Ra of the surface remote from the release layer 16 of the extremely-thin copper layer 18 was 3.5 nm. The composition of each layer other than the adhesive metal layer 14 a was substantially the same as that in Example 1. The adhesive metal layer 14 a has a composition of 98.0 atom % Cr and 2.0 atom % O.

Example 4

A copper foil provided with a carrier was prepared and evaluated as in Example 1 except that a carrier 12 of an alumina plate (product name: A-476, manufactured by Kyocera Corporation) having a surface with an arithmetic average roughness Ra of 0.2 μm and a thickness of 1000 μm was prepared, so that the surface was treated by chemical mechanical polishing (CMP) into the surface with an arithmetic average roughness Ra of 1.0 nm. The results are shown in Table 2. The arithmetic average roughness Ra of the surface remote from the release layer 16 of the extremely-thin copper layer 18 was 2.1 nm. The composition of each layer was substantially the same as that in Example 1.

Example 5

A copper foil provided with a carrier was prepared and evaluated as in Example 1 except that a carrier 12 of an yttria-stabilized zirconia plate (yttrium oxide 10 wt %) having a surface with an arithmetic average roughness Ra of 1.0 nm and having a thickness of 500 μm (manufactured by Shinkosha Co., Ltd.) was prepared. The results are shown in Table 2. The arithmetic average roughness Ra of the surface remote from the release layer 16 of the extremely-thin copper layer 18 was 2.2 nm. The composition of each layer was substantially the same as that in Example 1.

Example 6 (Comparative)

A copper foil provided with a carrier was prepared and evaluated as in Example 1 except that the adhesive metal layer 14 a and the release assisting layer 14 b were not formed. The results are shown in Table 2. The arithmetic average roughness Ra of the surface remote from the release layer 16 of the extremely-thin copper layer 18 was 1.0 nm. The composition of each layer was substantially the same as that in Example 1.

Example 7 (Comparative)

A copper foil provided with a carrier was prepared and evaluated as in Example 1 except that an aluminum sputtering target (purity: 99.999%) was used to form an aluminum layer instead of a titanium layer as the adhesive metal layer 14 a. The results are shown in Table 2. The arithmetic average roughness Ra of the surface remote from the release layer 16 of the extremely-thin copper layer 18 was 4.0 nm. The composition of each layer other than the adhesive metal layer 14 a was substantially the same as that in Example 1. The adhesive metal layer 14 a has a composition of 98 atom % Al and 2 atom % O.

Example 8 (Comparative)

A copper foil provided with a carrier was prepared and evaluated as in Example 1 except that the release assisting layer 14 b was not formed. The results are shown in Table 2. The arithmetic average roughness Ra of the surface remote from the release layer 16 of the extremely-thin copper layer 18 was 2.2 nm. The composition of each layer was substantially the same as that in Example 1

Example 9 (Comparative)

A copper foil provided with a carrier was prepared and evaluated as in Example 1 except that the release assisting layer 14 a was not formed. The results are shown in Table 2. The arithmetic average roughness Ra of the surface remote from the release layer 16 of the extremely-thin copper layer 18 was 3.1 nm. The composition of each layer was substantially the same as that in Example 1

Example 10 (Comparative)

A copper foil provided with a carrier was prepared and evaluated as in Example 1 except that a nickel sputtering target (purity: 99.999%) was used to form a nickel layer instead of a copper layer as the release assisting layer 14 b. The results are shown in Table 2. The arithmetic average roughness Ra of the surface remote from the release layer 16 of the extremely-thin copper layer 18 was 2.5 nm. The composition of each layer other than the release assisting layer 14 b was substantially the same as that in Example 1. The release assisting layer 14 b has a composition of 99.0 atom % Ni and 1.0 atom % O.

Example 11 to 13

Copper foils provided with carriers were prepared and evaluated as in Example 1 except that a molybdenum layer (Example 11), a tungsten layer (Example 12) and a manganese layer (Example 13) were formed by sputtering in place of the titanium layer as the adhesive metal layer 14 a. The results are shown in Table 2.

Examples 14 to 24 (Examples 18 and 19 are Comparative)

Copper foils provided with carriers were prepared and evaluated as in Example 1 except that intermediate alloy layers having the compositions shown in Table 3 were formed as a single layer structure consisting of the interlayer 14 instead of the two-layer structure consisting of the adhesive metal layer 14 a and the release assisting layer 14 b. The results are shown in Table 3.

Examples 25 to 29

Copper foils provided with carriers were prepared and evaluated as in Example 1 except that i) an adhesive metal layer 14 a, an release assisting layer 14 b, an antireflective layer 17, and an extremely-thin copper layer 18 were formed without masking the end face of the carrier 12, and ii) a release layer 16 with a variable thickness (end face thickness) was formed using a stainless steel plate for masking. As a result, the thickness (end face thickness) of each layer at the end face of the carrier 12 was as shown below.

-   -   Adhesive metal layer 14 a: titanium layer (end surface         thickness: 35 nm)     -   Release assisting layer 14 b: copper layer (end face thickness:         35 nm)     -   Release layer 16: Carbon layer (various end face thicknesses         shown in Table 4)     -   Antireflective layer 17: titanium layer (end face thickness: 38         nm)     -   Extremely-thin copper layer 18: copper layer (end face         thickness: 100 nm)

Example 30

A copper foil provided with a carrier was prepared and evaluated as in Example 1 except that i) an interlayer 14 as an intermediate alloy layer, a antireflective layer 17, and an extremely-thin copper layer 18 were formed without masking the end face of the carrier 12, and ii) a release layer 16 with a thickness (end face thickness) described below was formed using a stainless steel plate for masking.

-   -   Interlayer 13 (intermediate alloy layer): Cu—Mn alloy layer         (elemental ratio Cu:Mn=95:5, end surface thickness: 35 nm)     -   Release layer 16: carbon layer (end face thickness: 0 nm)     -   Antireflective layer 17: titanium layer (end face thickness: 38         nm)     -   Extremely-thin copper layer 18: copper layer (end face         thickness: 100 nm)

Evaluations on Various Items

The copper foil provided with a carrier of each of Examples 1 to 30 was subjected to evaluation on the following items. The results are shown in Tables 2 to 4.

<Evaluation 1: Peeling Resistance of Extremely-Thin Copper Layer Against Developer>

The surface of the extremely-thin copper layer of each copper foil provided with a carrier was treated with dilute sulfuric acid of 0.05 mol/L to remove the oxide film on the surface, followed by washing with water and drying. Then, a photosensitive dry film was attached to the surface of the extremely-thin copper layer, and exposed and developed such that a pattern of line/space (L/S)=5 μm/5 μm is given. Development was carried out by showering at 25° C. for 2 min using an aqueous 1.0 wt % sodium carbonate developer. The presence of peeling (or degree of separation) of the extremely-thin copper layer due to infiltration of the developer into the interface between the extremely-thin copper layer and the carrier (especially between the release layer and the adhesive metal layer) after the development was evaluated.

The results were rated based on the following criteria.

Rank AA: No peeling of the extremely-thin copper layer was observed.

Rank A: Peeling with a size of 3 μm or less in diameter was observed.

Rank B: Peeling with a size of 50 μm or less in diameter was observed.

Rank C: Peeling with a size larger than 50 μm in diameter was observed.

<Evaluation 2: Peelability Between Carrier and Extremely-Thin Copper Layer>

The peel strength of the copper foil provided with a carrier was measured after a thermal history of solder reflow and vacuum heat press. After panel electrolytic copper plating having a thickness of 18 μm on the side adjacent the extremely-thin copper layer 18 of the copper foil 10 provided with a carrier, the sample was heat-treated by solder reflow (kept at 260° C. or higher for 2 min) (thermal history 1), assuming mount of electronic components, and the copper foil was spontaneously cooled to room temperature. Thereafter, the copper foil was pressed at a temperature of 220° C. for 90 min under a pressure of 30 kgf/cm² (thermal history 2). The peel strength (gf/cm) of the resulting copper-clad laminate was measured by peeling off the electrolytic copper plating layer integrated with the extremely-thin copper layer 18 (measuring area: 50 mm×20 mm) in accordance with JIS C 6481-1996. The resulting peel strength (average value) was rated based on the following criteria.

Rank A: peel strength of 2 to 10 gf/cm

Rank B: peel strength of 1 to 30 gf/cm (except for 2 to 10 gf/cm)

Rank C: peel strength of less than 1 gf/cm or greater than 30 gf/cm

<Evaluation 3: Evaluation of Film Chipping at Side Ends of Coreless Support>

Electrolytic copper plating was applied to the coreless support used in Evaluation 1, followed by flash etching of the resultant extremely-thin copper layer with a sulfuric acid-hydrogen peroxide solution to form a coreless support with a wiring pattern. The maximum width (mm) of chipping of the film (i.e., extremely-thin copper layer and antireflective layer) on the release layer at the side ends of each coreless support provided with a wiring pattern was measured to be rated based on the following criteria. The results are shown in Tables 2 to 4.

-   -   Rank AA: Less than 0.1 mm (best)     -   Rank A: 0.1 mm or more and less than 1 mm (good)     -   Rank B: 1 mm or more and less than 2 mm (acceptable)     -   Rank C: 2 mm or more (unacceptable)

<Evaluation 4: Evaluation of Fine Pattern Formability of Embedded Wiring Layer>

A prepreg and a copper foil were laminated in this order on the coreless support provided with the wiring pattern prepared in Evaluation 3 and cured into a laminate with a build-up layer. The laminate with a build-up layer was mechanically separated at the release layer to prepare a multilayer wiring board including the build-up layer. The antireflective layer was subjected to flash etching under the conditions shown in Table 1, and the properties of the wiring layer embedded in the build-up layer were observed to be ranked based on the following criteria. The results are shown in Tables 2 and 3. One piece was defined as 8 mm×8 mm square and the number of observation pieces in each example was set to 336 to count the number of defective pieces in the embedded wiring. The defective mode includes, for example, shortcutting due to peeling of the extremely-thin copper layer and peelings of the adhesive metal layer and the release assisting layer, which leave metal adjacent to the carrier when the coreless support is peeled.

-   -   Rank AA: percent defective is less than 5% by number (best)     -   Rank A: percent defective is 5% or more and less than 10% by         number (good)     -   Rank B: percent defective rate is 10% or more and 20% or less by         number (acceptable)     -   Rank C: percent defective is 20% or more and less than 50% by         number (unacceptable)

<Evaluation 5: Evaluation of Chemical Penetration Depth>

A prepreg having a size of 100 mm×100 mm (FR-4 manufactured by Panasonic Corporation, 200 μm thick) was laminated on the coreless support with a wiring pattern prepared in Evaluation 3 to cure the prepreg into a printed wiring board. The printed wiring board was subjected to desmear treatment using a sodium permanganate solution, and the chemical penetration depth (mm) was measured as an indication of the penetrated amount of chemical solution.

This desmear treatment was carried out by the following procedures using the process solution shown below (manufactured by Rohm and Haas Electronic Materials LLC).

[Swelling Process]

-   -   Process solution: Circuposit MLB Conditioner 211 (120 mL/L) and         -   Circuposit Z (100 mL/L)     -   Process conditions: immersion for 5 min at 75° C.

[Permanganic Acid Process]

-   -   Process solution: Circuposit MLB promoter 213A (110 mL/L) and         -   Circuposit MLB promoter 213 B (150 mL/L)     -   Process conditions: immersion for 5 min at 80° C.

[Neutralization Process]

-   -   Process solution: Circuposit MLB Neutralizer 216-2 (200 mL/L)     -   Process conditions: immersion for 5 min at 45° C.

The measured chemical penetration depth (mm) was rated based on the following criteria. The results are shown in Tables 2 to 4.

-   -   Rank AA: less than 0.1 mm (best)     -   Rank A: 0.1 mm or more and less than 0.5 mm (good)     -   Rank B: 0.5 mm or more and less than 2 mm (acceptable)     -   Rank C: 2 mm or more (unacceptable)

TABLE 2 Chipping width Percent Peeling of defective resistance Releasability extremely-thin in pattern Interlayer of extremely-thin of carrier copper layer Chemical formation of Adhesive Release copper layer Peel and other layers penetration embedded metal assisting against developer strength at side ends depth wiring layer Carrier layer layer (μm) (gf/cm) Rank (mm) (mm) (% by number) Ex. 1 Glass Ti Cu  0(AA) 5.1 A 1.0(B)  0(AA)  0(AA) Ex. 2 Glass Ni Cu  2(A) 3.5 A 1.3(B) 1.0(B)  9(A) Ex. 3 Glass Cr Cu  1(A) 2.0 A 1.0(B) 0.7(B) 10(A) Ex. 4 Alumina Ti Cu  0(AA) 11.5  B 1.2(B) 1.0(B) 14(B) Ex. 5 Zirconia Ti Cu  0(AA) 1.5 B 1.5(B) 1.8(B) 13(B) Ex. 6* Glass None None  2(A) Less than 1 B 3.5(C) 2.5(C) 45(C) Ex. 7* Glass Al Cu 97(C) Non-peelable C 2.5(C) 3.0(C) — Ex. 8* Glass Ti None  1(A) Non-peelable C 1.4(B) 1.4(B) — Ex. 9* Glass None Cu  2(A) Non-peelable C 2.5(C) 4.0(C) — Ex. 10* Glass Ti Ni  3(A) Non-peelable C 1.0(B) 1.2(B) — Ex. 11 Glass Mo Cu  0(AA) 5.5 A 1.0(B) 1.0(B)  2(AA) Ex. 12 Glass W Cu  0(AA) 4.3 A 1.0(B) 0.5(B) 10(A) Ex. 13 Glass Mn Cu  0(AA) 10.0  B 1.0(B) 0.7(B)  4(AA) *denotes comparative examples. “—” in the table indicates impossible evaluation of the pattern formability of the embedded wiring layer due to “non-peelable” carrier.

TABLE 3 Chipping width Percent Peeling of defective resistance extremely-thin in pattern of extremely-thin Releasability copper layer Chemical formation of copper layer of carrier and other layers penetration embedded Interlayer against developer Peel strength at side ends depth wiring layer Carrier Intermediate alloy layer (μm) (gf/cm) Rank (mm) (mm) (% by number) Ex. 14 Glass Cu—Mn (ratio 95:5) 0(AA) 5.0 A 1.0(B)   0(AA)  4(AA) Ex. 15 Glass Cu—Mn (ratio 99:1) 1(A)    4.6 A 1.0(B) 1.5(B) 17(B) Ex. 16 Glass Cu—Mn (ratio 90:10) 0(AA) 4.4 A 1.0(B)   0(AA)  3(AA) Ex. 17 Glass Cu—Mn (ratio 70:30) 0(AA) 4.8 A 1.0(B)   0(AA)  5(AA) Ex. 18 Glass Cu—Ag (ratio 95:5) 0(AA) 5.2 A 3.5(C)   0(AA) 15(B) Ex. 19 Glass Cu—Al (ratio 95:5) 100(C)    3.8 A 3.0(C) 3.0(C) 30(C) Ex. 20 Glass Cu—Cr (ratio 95:5) 0(AA) 4.9 A 1.5(8) 1.2(B)  9(A) Ex. 22 Glass Cu—Ti (ratio 95:5) 0(AA) 4.5 A 1.0(8)   0(AA)  4(AA) Ex. 23 Glass Cu—Mo (ratio 95:5) 0(AA) 5.2 A 1.3(B) 1.2(B)  3(AA) Ex. 24 Glass Cu—W (ratio 95:5) 0(AA) 5.3 A 1.0(B) 1.6(B)  8(A) * denotes comparative examples. The ratio is based on the number of atoms

TABLE 4 Thickness of Chipping width of release layer at extremely-thin copper Chemical Interlayer carrier end face layer and other penetration (Adhesive metal layer/Release (end-face thickness) layers at side ends depth assisting layer) (nm) (mm) (mm) Ex. 25 Double-layer (Ti layer/Cu layer) 0 Ex. 26 Double-layer (Ti layer/Cu layer) 0.3 0 (AA) 0 (AA) Ex. 27 Double-layer (Ti layer/Cu layer) 0.9 0.5 (A) 0.2 (A) Ex. 28 Double-layer (Ti layer/Cu layer) 1.5 15 (B) 1.5 (B) Ex. 29 Double-layer (Ti layer/Cu layer) 3 (same 1.5 (B) 5.0 (B) thickness as surface) Ex. 30 Single-layer (Cu—Mn alloy layer, 0 0 (AA) 0 (AA) element ratio 95:5) 

What is claimed is:
 1. A method for manufacturing a printed wiring board, the method comprising: providing a copper foil including a carrier as a support; wherein the copper foil provided with a carrier comprises: a carrier; an interlayer disposed on the carrier, the interlayer containing at least one metal selected from the group consisting of Ti, Cr, Mo, Mn, W, and Ni; a release layer disposed on the interlayer; an extremely-thin copper layer disposed on the release layer; and an antireflective layer disposed between the release layer and the extremely-thin copper layer, forming a wiring layer on a surface of the extremely-thin copper layer to prepare a coreless support including a wiring layer; forming a build-up layer on a surface having the wiring layer of the coreless support including the wiring layer; mounting an electronic element on the coreless support to prepare a laminate; separating the laminate to prepare a multilayer wiring board including the build-up layer; performing selective etching of the antireflective layer to expose a wiring layer of the multilayer wiring board; and providing an outer layer pad on a surface of the wiring layer.
 2. The method for manufacturing a printed wiring board according to claim 1, wherein the carrier is composed of glass or ceramics.
 3. The method for manufacturing a printed wiring board according to claim 1, wherein each of the interlayer, the release layer, and the extremely-thin copper layer are formed by sputtering. 